| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12681151-12681365 | Rare:55 | ||||
| chr19:12681441-12682105 | Common:6; Rare:300; Clinvar (pathogenic):1 | ||||
| chr19:12696560-12696767 | Rare:94 | ||||
| chr19:12722000-12722093 | Rare:19 | ||||
| chr19:12722216-12722347 | Rare:20 | ||||
| chr19:12722446-12722896 | Common:4; Rare:89 | ||||
| chr19:12722958-12723092 | Rare:30 | ||||
| chr19:12723863-12724129 | Common:1; Rare:63 | ||||
| chr19:12734373-12734461 | Rare:21 | ||||
| chr19:12734580-12734908 | Common:1; Rare:122 | ||||
| chr19:12736816-12736938 | Common:1; Rare:30 | ||||
| chr19:12737120-12737571 | Common:1; Rare:112 | ||||
| chr19:12775496-12775806 | Common:3; Rare:84 | ||||
| chr19:12778012-12778338 | Common:1; Rare:65 | ||||
| chr19:12778415-12778630 | Rare:37 |